临床试验
嵌合抗原受体
CD19
仿形(计算机编程)
计算生物学
医学
计算机科学
生物信息学
T细胞
免疫学
生物
抗原
免疫系统
操作系统
作者
Daiyan Zhang,Liyang Lyu,Shuo Han,Jiaqi Xu,Guang Hu,Qi Zhao,Hu Y
标识
DOI:10.1016/j.intimp.2023.111273
摘要
Since the approval of the first chimeric antigen receptor (CAR)-T product in 2017, the number of new CAR-T clinical trials worldwide exceeds 100 per year. 1649 clinical studies have been conducted to explore possible future clinical applications of targets or target pairs through different biotechnologies. In this study, we aim to take a data-driven analytical approach to explore potential dual-target pairs based on clinical trial information. We screened 1283 non-withdrawal interventional CAR-T clinical trials spanning 96 different targets and 74 target pairs from clinicaltrials.gov. Through the Circos plot and temporal network plots, the information between targets and indications was visualized. Based on the assumption that two targets of a target pair must target the same indication, five new target pairs were inferred, including CD19/CD7, CD19/CD5, CD19/CD37, and CD19/BAFFR and validated by expression pattern, literature and patent information. This study provides novel support for target profiling of CAR-T from the perspective of clinical trials and also provides a reference for researchers and developers to select new targets or target pairs of CAR-T cell therapy.
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